A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17451060



Internal ID22508933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:96892137..97019082hg38UCSC Ensembl
chrX:96147136..96274081hg19UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg38126946
hg19126946
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5872839
Supporting Variants
Samples
Known GenesDIAPH2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17451060
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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